SG192685A1 - Low-tack, hydrophobic ophthalmic device materials - Google Patents
Low-tack, hydrophobic ophthalmic device materials Download PDFInfo
- Publication number
- SG192685A1 SG192685A1 SG2013060389A SG2013060389A SG192685A1 SG 192685 A1 SG192685 A1 SG 192685A1 SG 2013060389 A SG2013060389 A SG 2013060389A SG 2013060389 A SG2013060389 A SG 2013060389A SG 192685 A1 SG192685 A1 SG 192685A1
- Authority
- SG
- Singapore
- Prior art keywords
- device material
- acrylate
- copolymeric
- monomer
- formula
- Prior art date
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- 239000000463 material Substances 0.000 title claims abstract description 114
- 230000002209 hydrophobic effect Effects 0.000 title claims abstract description 15
- 239000000178 monomer Substances 0.000 claims abstract description 73
- 229920001400 block copolymer Polymers 0.000 claims abstract description 22
- -1 poly(ethylene glycol) Polymers 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 30
- 229920001223 polyethylene glycol Polymers 0.000 claims description 30
- 229920001577 copolymer Polymers 0.000 claims description 28
- HPSGLFKWHYAKSF-UHFFFAOYSA-N 2-phenylethyl prop-2-enoate Chemical compound C=CC(=O)OCCC1=CC=CC=C1 HPSGLFKWHYAKSF-UHFFFAOYSA-N 0.000 claims description 18
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical group CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 15
- 239000006096 absorbing agent Substances 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 12
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 12
- 238000004132 cross linking Methods 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 7
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 6
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 claims description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 5
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims description 5
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 229910000077 silane Inorganic materials 0.000 claims description 5
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims description 4
- RHOOUTWPJJQGSK-UHFFFAOYSA-N 2-phenylsulfanylethyl prop-2-enoate Chemical compound C=CC(=O)OCCSC1=CC=CC=C1 RHOOUTWPJJQGSK-UHFFFAOYSA-N 0.000 claims description 4
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- RKFUZDIZLQCJKA-UHFFFAOYSA-N [dimethyl(phenyl)silyl]methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC[Si](C)(C)C1=CC=CC=C1 RKFUZDIZLQCJKA-UHFFFAOYSA-N 0.000 claims description 3
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims description 2
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 claims description 2
- ROJWTNWAEYEKMO-UHFFFAOYSA-N 2-phenylmethoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCC1=CC=CC=C1 ROJWTNWAEYEKMO-UHFFFAOYSA-N 0.000 claims description 2
- HTWRFCRQSLVESJ-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOC(=O)C(C)=C HTWRFCRQSLVESJ-UHFFFAOYSA-N 0.000 claims description 2
- NWBTXZPDTSKZJU-UHFFFAOYSA-N 3-[dimethyl(trimethylsilyloxy)silyl]propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](C)(C)O[Si](C)(C)C NWBTXZPDTSKZJU-UHFFFAOYSA-N 0.000 claims description 2
- JRJNSEMUYTUGLA-UHFFFAOYSA-N 3-phenoxypropyl prop-2-enoate Chemical compound C=CC(=O)OCCCOC1=CC=CC=C1 JRJNSEMUYTUGLA-UHFFFAOYSA-N 0.000 claims description 2
- SJOIDEGZPXSHOC-UHFFFAOYSA-N 3-phenylmethoxypropyl prop-2-enoate Chemical compound C=CC(=O)OCCCOCC1=CC=CC=C1 SJOIDEGZPXSHOC-UHFFFAOYSA-N 0.000 claims description 2
- PKBZUGSITIBLFK-UHFFFAOYSA-N 3-phenylpropyl prop-2-enoate Chemical compound C=CC(=O)OCCCC1=CC=CC=C1 PKBZUGSITIBLFK-UHFFFAOYSA-N 0.000 claims description 2
- BESKSSIEODQWBP-UHFFFAOYSA-N 3-tris(trimethylsilyloxy)silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C BESKSSIEODQWBP-UHFFFAOYSA-N 0.000 claims description 2
- MXNDNUJKPFXJJX-UHFFFAOYSA-N 4-phenylbutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCC1=CC=CC=C1 MXNDNUJKPFXJJX-UHFFFAOYSA-N 0.000 claims description 2
- FBOYEYXUKAKVDL-UHFFFAOYSA-N 5-phenylpentyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCC1=CC=CC=C1 FBOYEYXUKAKVDL-UHFFFAOYSA-N 0.000 claims description 2
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- UIUXUFNYAYAMOE-UHFFFAOYSA-N methylsilane Chemical compound [SiH3]C UIUXUFNYAYAMOE-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 17
- 239000000654 additive Substances 0.000 abstract description 6
- 230000000996 additive effect Effects 0.000 abstract description 6
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
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- 238000000034 method Methods 0.000 description 6
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- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 5
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000012632 extractable Substances 0.000 description 4
- NFRBUOMQJKUACC-UHFFFAOYSA-N triethyl(pentyl)azanium Chemical compound CCCCC[N+](CC)(CC)CC NFRBUOMQJKUACC-UHFFFAOYSA-N 0.000 description 4
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- WFRLANWAASSSFV-FPLPWBNLSA-N palmitoleoyl ethanolamide Chemical compound CCCCCC\C=C/CCCCCCCC(=O)NCCO WFRLANWAASSSFV-FPLPWBNLSA-N 0.000 description 3
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- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000671 polyethylene glycol diacrylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229940042596 viscoat Drugs 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Materials For Medical Uses (AREA)
- Prostheses (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Eyeglasses (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Silicon Polymers (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161440633P | 2011-02-08 | 2011-02-08 | |
| US201161493654P | 2011-06-06 | 2011-06-06 | |
| PCT/US2012/024125 WO2012109228A1 (en) | 2011-02-08 | 2012-02-07 | Low-tack, hydrophobic ophthalmic device materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG192685A1 true SG192685A1 (en) | 2013-09-30 |
Family
ID=45774329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2013060389A SG192685A1 (en) | 2011-02-08 | 2012-02-07 | Low-tack, hydrophobic ophthalmic device materials |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8969429B2 (es) |
| EP (1) | EP2673666B1 (es) |
| JP (1) | JP5868430B2 (es) |
| KR (1) | KR101729641B1 (es) |
| CN (1) | CN103348266B (es) |
| AR (1) | AR085320A1 (es) |
| AU (1) | AU2012214565B2 (es) |
| BR (1) | BR112013020024A2 (es) |
| CA (1) | CA2825359C (es) |
| ES (1) | ES2531339T3 (es) |
| HK (1) | HK1187415A1 (es) |
| IL (1) | IL227372A (es) |
| MX (1) | MX346220B (es) |
| RU (1) | RU2570575C2 (es) |
| SG (1) | SG192685A1 (es) |
| TW (1) | TWI517861B (es) |
| WO (1) | WO2012109228A1 (es) |
| ZA (1) | ZA201305156B (es) |
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| TWI513768B (zh) * | 2011-06-01 | 2015-12-21 | Novartis Ag | 疏水性丙烯酸系眼內水晶體材料 |
| US9188702B2 (en) * | 2011-09-30 | 2015-11-17 | Johnson & Johnson Vision Care, Inc. | Silicone hydrogels having improved curing speed and other properties |
| CA2881988C (en) * | 2012-10-15 | 2018-01-23 | Novartis Ag | High refractive index ophthalmic device materials with reduced tack |
| EP3077016B1 (en) * | 2013-12-04 | 2018-05-16 | Novartis AG | Soft acrylic materials with high refractive index and minimized glistening |
| WO2015170278A1 (en) * | 2014-05-07 | 2015-11-12 | Tubitak | A formulation and lens manufacturing process for the production of intraocular lens (iol) |
| US9864102B2 (en) | 2014-12-16 | 2018-01-09 | Novartis Ag | Hydrophobic acrylate-acrylamide copolymers for ophthalmic devices |
| CA2965742C (en) * | 2014-12-16 | 2019-10-01 | Novartis Ag | Low-water content acrylate-acrylamide copolymers for ophthalmic devices |
| EP4245327A3 (en) * | 2015-06-10 | 2023-12-27 | Alcon Inc. | Intraocular lens materials and components |
| US20210322152A1 (en) * | 2020-04-15 | 2021-10-21 | Rxsight, Inc. | Composite light adjustable intraocular lens with adhesion promoter |
| TW201927263A (zh) | 2017-12-18 | 2019-07-16 | 瑞士商諾華公司 | 觸覺力分佈得到改善的眼內透鏡平台 |
| TW201927262A (zh) | 2017-12-20 | 2019-07-16 | 瑞士商諾華公司 | 具有前偏置光學設計之眼內透鏡 |
| JP6784720B2 (ja) * | 2018-06-01 | 2020-11-11 | 上海富吉医療器械有限公司Ｓｈａｎｇｈａｉ Ｃｈａｒｔｗｅｌｌ Ｍｅｄｉｃａｌ Ｉｎｓｔｒｕｍｅｎｔ Ｃｏ．， Ｌｔｄ． | ポリマー材料および眼内レンズ |
| CN109898176B (zh) * | 2019-02-01 | 2021-07-02 | 东华大学 | 一种柔性可拉伸水凝胶光导纤维传感器及其制备和应用 |
| US20220143267A1 (en) * | 2019-03-07 | 2022-05-12 | Teleon Holding B.V. | Intraocular lens compositions |
| US11708440B2 (en) | 2019-05-03 | 2023-07-25 | Johnson & Johnson Surgical Vision, Inc. | High refractive index, high Abbe compositions |
| US11667742B2 (en) | 2019-05-03 | 2023-06-06 | Johnson & Johnson Surgical Vision, Inc. | Compositions with high refractive index and Abbe number |
| CN116925281A (zh) * | 2019-12-24 | 2023-10-24 | 爱博诺德(北京)医疗科技股份有限公司 | 眼科材料及其制备方法 |
| CN113021738B (zh) * | 2019-12-24 | 2023-06-27 | 烟台爱博诺德医用材料有限公司 | 眼科材料的制备方法 |
| JP2023547481A (ja) | 2020-10-29 | 2023-11-10 | ジョンソン・アンド・ジョンソン・サージカル・ビジョン・インコーポレイテッド | 高い屈折率及びアッベ数を有する組成物 |
| TWI793944B (zh) * | 2021-12-24 | 2023-02-21 | 永勝光學股份有限公司 | 過濾藍光之眼用鏡片及過濾藍光之眼用鏡片的製作方法 |
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-
2012
- 2012-02-06 TW TW101103752A patent/TWI517861B/zh not_active IP Right Cessation
- 2012-02-07 ES ES12706743T patent/ES2531339T3/es active Active
- 2012-02-07 US US13/367,914 patent/US8969429B2/en active Active
- 2012-02-07 KR KR1020137020965A patent/KR101729641B1/ko active IP Right Grant
- 2012-02-07 CA CA2825359A patent/CA2825359C/en not_active Expired - Fee Related
- 2012-02-07 EP EP12706743.7A patent/EP2673666B1/en active Active
- 2012-02-07 RU RU2013141209/04A patent/RU2570575C2/ru not_active IP Right Cessation
- 2012-02-07 JP JP2013552728A patent/JP5868430B2/ja active Active
- 2012-02-07 CN CN201280007928.1A patent/CN103348266B/zh not_active Expired - Fee Related
- 2012-02-07 AU AU2012214565A patent/AU2012214565B2/en not_active Ceased
- 2012-02-07 BR BR112013020024A patent/BR112013020024A2/pt not_active Application Discontinuation
- 2012-02-07 AR ARP120100394A patent/AR085320A1/es not_active Application Discontinuation
- 2012-02-07 MX MX2013009141A patent/MX346220B/es active IP Right Grant
- 2012-02-07 WO PCT/US2012/024125 patent/WO2012109228A1/en active Application Filing
- 2012-02-07 SG SG2013060389A patent/SG192685A1/en unknown
-
2013
- 2013-07-08 IL IL227372A patent/IL227372A/en not_active IP Right Cessation
- 2013-07-09 ZA ZA2013/05156A patent/ZA201305156B/en unknown
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2014
- 2014-01-10 HK HK14100338.5A patent/HK1187415A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2012214565A1 (en) | 2013-07-25 |
| BR112013020024A2 (pt) | 2017-12-12 |
| HK1187415A1 (en) | 2014-04-04 |
| TW201235051A (en) | 2012-09-01 |
| TWI517861B (zh) | 2016-01-21 |
| KR101729641B1 (ko) | 2017-04-24 |
| AU2012214565B2 (en) | 2014-11-20 |
| AR085320A1 (es) | 2013-09-25 |
| US8969429B2 (en) | 2015-03-03 |
| CN103348266B (zh) | 2016-05-04 |
| ES2531339T3 (es) | 2015-03-13 |
| RU2570575C2 (ru) | 2015-12-10 |
| MX346220B (es) | 2017-03-09 |
| EP2673666A1 (en) | 2013-12-18 |
| CA2825359A1 (en) | 2012-08-16 |
| CA2825359C (en) | 2018-07-31 |
| US20120202916A1 (en) | 2012-08-09 |
| NZ612852A (en) | 2015-01-30 |
| ZA201305156B (en) | 2014-09-25 |
| JP2014506814A (ja) | 2014-03-20 |
| IL227372A0 (en) | 2013-09-30 |
| WO2012109228A1 (en) | 2012-08-16 |
| MX2013009141A (es) | 2013-10-01 |
| KR20140051125A (ko) | 2014-04-30 |
| EP2673666B1 (en) | 2014-12-31 |
| IL227372A (en) | 2016-02-29 |
| JP5868430B2 (ja) | 2016-02-24 |
| RU2013141209A (ru) | 2015-03-20 |
| CN103348266A (zh) | 2013-10-09 |
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